Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing melamine salt of bis(pentaerythritol phosphate) phosphoric acid

a technology of pentaerythritol phosphate and melamine salt, which is applied in the field of preparing a melamine salt of bis (pentaerythritol phosphate) phosphoric acid, can solve the problems of numerous limitations on the selection of reaction solvents, the inability to recollect phosphorus oxychloride liquid, and the high molar ratio of excessive phosphorus oxychloride to be used for the reaction

Inactive Publication Date: 2008-10-16
CHANG CHUN PLASTICS
View PDF5 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010]It is another object of the present invention to provide a method for producing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid, which can shorten the esterification time.
[0011]It is still another object of the present invention to provide a method for producing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid, which can improve the the reaction system in safety aspect.
[0012]In accordance with the foregoing and other objectives, the present invention proposes a method for producing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid. The method includes carrying out an esterification reaction in an extruder, of which pentaerythritol and diphosphorous pentaoxide are mixed to react with each other to form bis(pentaerythritol phosphate) phosphoric acid; and then carrying out a quaternization reaction by mixing and reacting bis(pentaerythritol phosphate) phosphoric acid, which is formed in the esterification reaction in the presence of a solvent, with melamine or a derivative thereof, followed by removing water to obtain a melamine salt of bis(pentaerythritol phosphate) phosphoric acid. In the method of the present invention, diphosphorous pentoxide is used as a reactant. The use of the method is free of generating hydrogen chloride as waste gas or creating the need to recollect trichlorophosphoric acid. Moreover, esterification can be carried out without the need to use organic solvents, such that the esterification time can be shortened and a high pressure in a closed reaction system that causes explosion can be avoided.

Problems solved by technology

Further, because the viscosity of resin in the reaction is high, a high molar ratio of an excessive amount phosphorus oxychloride must be used for the reaction.
Thus, the need to recollect phosphorus oxychloride liquid becomes another drawback in the method.
This poses numerous limitations on the selection of reaction solvents.
This leads to an increased pressure in the closed system, thereby causing a safety issue.
Moreover, the viscosity of pentaerythritol in the molten state is extremely high, which makes it difficult to agitate pentaerythritol.
Therefore, a longer reaction time is required.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing melamine salt of bis(pentaerythritol phosphate) phosphoric acid

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0019]Diphosphorous pentaoxide (P2O5) and pentaerythritol (PE) were fed into a double-screw extruder at a molar ratio of 1:1. Esterification was performed at a rotation speed of 100 min−1 and a sleeve temperature in the range of 30 to 200° C. to obtain bis(pentaerythritol phosphate) phosphoric acid. Sampling was made at the outlet of the extruder, and a 31P-NMR map was used to calculate the esterifying rate. The result was recorded in Table 1.

[0020]An amount of 122.4 g of bis(pentaerythritol ester) phosphate, 111 g of melamine, and 500 g of pure water was added into a 1000 mL beaker, and the reacting temperature was increased to 90° C. while stirring. The duration of the process was 30 minutes. Then, the reacting temperature was decreased to 25° C. to remove water by filtration. A melamine salt of bis(pentaerythritol phosphate) phosphoric acid was obtained after baking.

example 2-3

[0021]Steps in EXAMPLE 1 were repeated, and the screw rotation speed of the double-screw extruder was adjusted to carry out esterification according to Table 1. Sampling was made at the outlet of the extruder, and a 31P-NMR map was used to calculate the esterifying rate. The results were recorded in Table 1.

example 4

[0022]Steps in EXAMPLE 1 were repeated, and the screw rotation speed of the double-screw extruder was adjusted to carry out esterification according to Table 1. Sampling was made at the outlet of the extruder, and a 31P-NMR map was used to calculate the esterifying rate. The result was recorded in Table 1.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
molar ratioaaaaaaaaaa
molar ratioaaaaaaaaaa
temperatureaaaaaaaaaa
Login to View More

Abstract

A method for producing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid is proposed. The method includes the steps of reacting and mixing pentaerythritol and diphosphorous pentaoxide in an extruder to carry out esterification to produce bis(pentaerythritol phosphate) phosphoric acid; and mixing bis(pentaerythritol phosphate) phosphoric acid with melamine or a derivative thereof to carry out quaternization in the presence of a solvent, followed by removing water to obtain a melamine salt of bis(pentaerythritol phosphate) phosphoric acid. Diphosphorous pentaoxide is used in the method as a reactant, so that no hydrogen chloride is produced and it is not necessary to recollect trichlorophosphoric acid. Moreover, in the method of the present invention, such that esterification time can be shortened and a high pressure in a closed reaction system that causes explosion can be avoided.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims the benefit of Taiwan application no. 096112972, filed Apr. 13, 2007, the disclosure of which is incorporated herein by reference in its entirety.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention relates to methods for preparing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid, and more particularly, to a method for preparing a melamine salt of bis(pentaerythritol phosphate) phosphoric acid by esterifying pentaerythritol and diphosphorous pentoxide.[0004]2. Description of the Prior Art[0005]The melamine salt of bis(pentaerythritol phosphate) phosphoric acid has a cyclic structure, which exhibits excellent heat stability during the thermal gravimetric analysis and the differential thermal analysis. The melamine salt of bis(pentaerythritol phosphate) phosphoric acid can be used in polyolefine, polyurethane, poly(phenylene oxide) (PPO), poly(methacrylate) (PMMA), po...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): C07D251/12
CPCC07D251/18C07D251/56
Inventor HWANG, KUEN-YUANTU, AN-PANGCHEN, GAI-CHI
Owner CHANG CHUN PLASTICS
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products